1-Chloro-4-(chloromethyl)benzene → HCID 14423765, compound

HRID 569820Notes

Reaction equation

HRID 569820 reaction equation
[H-].[Na+].[O:3]=[C:4]1[NH:13][C:12](=[O:14])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]1[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17].[Cl:21][C:22]1[CH:29]=[CH:28][C:25]([CH2:26]Cl)=[CH:24][CH:23]=1>CN(C)C=O.C(OCC)(=O)C>[Cl:21][C:22]1[CH:29]=[CH:28][C:25]([CH2:26][N:13]2[C:12](=[O:14])[C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[N:5]([CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[C:4]2=[O:3])=[CH:24][CH:23]=1

Participants

6

Procedure

To a suspension of sodium hydride (60% in mineral oil, 367 mg) in N,N-dimethylformamide (15 ml) was added a solution of ethyl 2-(1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl)-acetate (2.0 g) in N,N-dimethylformamide (35 ml) with stirring at room temperature under nitrogem atmosphere, and the mixture was stirred at the same temperature for 15 minutes. To this mixture was added 4-chlorobenzyl chloride (1.48 g) with stirring at room temperature and the mixture was stirred at the same temperature for 1 hour. The solvent was evaporated in vacuo to give a residue, which was dissolved in ethyl acetate. The ethyl acetate solution was washed with water and dried. Evaporation of the solvent gave a residue, which was washed with n-hexane to afford ethyl 2-[3-(4-chlorobenzyl)-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetate (2.55 g).

Workup

  1. stirringthe mixture was stirred at the same temperature for 15 minutes
  2. stirringwith stirring at room temperature
  3. stirringthe mixture was stirred at the same temperature for 1 hour
  4. customThe solvent was evaporated in vacuo
  5. customto give a residue, which
  6. washThe ethyl acetate solution was washed with water
  7. customdried
  8. customEvaporation of the solvent
  9. customgave a residue, which
  10. washwas washed with n-hexane

Sources & evidence

ORD record
ord-486f2fbf9c4549488401857103857a45
Source dataset
uspto-grants-1988_03
Patent number
US04734419

Reaction notes

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